Lysophosphatidylcholine Regulates Sexual Stage Differentiation in the Human Malaria Parasite Plasmodium falciparum

Nicolas M. B. Brancucci(Harvard University), Joseph P. Gerdt(Harvard University), Chengqi Wang(University of South Florida), Mariana De Niz(Harvard University), Nisha Philip(Wellcome Centre for Molecular Parasitology), Swamy R. Adapa(University of South Florida), Min Zhang(University of South Florida), Eva Hitz(Swiss Tropical and Public Health Institute), Igor Niederwieser(Swiss Tropical and Public Health Institute), Sylwia D. Boltryk(Swiss Tropical and Public Health Institute), Marie-Claude N. Laffitte(Wellcome Centre for Molecular Parasitology), Martha A. Clark(Harvard University), Christof Grüring(Harvard University), Deepali Ravel(Harvard University), Alexandra Blancke Soares(Wellcome Centre for Molecular Parasitology), Allison Demas(Harvard University), Selina Bopp(Harvard University), Belén Rubio‐Ruíz(Universidad de Granada), Ana Conejo‐García(Universidad de Granada), Dyann F. Wirth(Harvard University), Edyta Gendaszewska‐Darmach(Lodz University of Technology), Manoj T. Duraisingh(Harvard University), John H. Adams(University of South Florida), Till S. Voss(Swiss Tropical and Public Health Institute), Andrew P. Waters(Wellcome Centre for Molecular Parasitology), Rays H. Y. Jiang(University of South Florida), Jon Clardy(Harvard University), Matthias Marti(Harvard University)
Cell
November 9, 2017
Cited by 383Open Access
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Abstract

Transmission represents a population bottleneck in the Plasmodium life cycle and a key intervention target of ongoing efforts to eradicate malaria. Sexual differentiation is essential for this process, as only sexual parasites, called gametocytes, are infective to the mosquito vector. Gametocyte production rates vary depending on environmental conditions, but external stimuli remain obscure. Here, we show that the host-derived lipid lysophosphatidylcholine (LysoPC) controls P. falciparum cell fate by repressing parasite sexual differentiation. We demonstrate that exogenous LysoPC drives biosynthesis of the essential membrane component phosphatidylcholine. LysoPC restriction induces a compensatory response, linking parasite metabolism to the activation of sexual-stage-specific transcription and gametocyte formation. Our results reveal that malaria parasites can sense and process host-derived physiological signals to regulate differentiation. These data close a critical knowledge gap in parasite biology and introduce a major component of the sexual differentiation pathway in Plasmodium that may provide new approaches for blocking malaria transmission.


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